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Lucie Rodriguez
Researcher at Science for Life Laboratory
Publications - 9
Citations - 1415
Lucie Rodriguez is an academic researcher from Science for Life Laboratory. The author has contributed to research in topics: Immune system & Autoantibody. The author has an hindex of 6, co-authored 8 publications receiving 467 citations.
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Journal ArticleDOI
The Immunology of Multisystem Inflammatory Syndrome in Children with COVID-19
Camila Rosat Consiglio,Nicola Cotugno,Nicola Cotugno,Fabian Sardh,Christian Pou,Donato Amodio,Donato Amodio,Lucie Rodriguez,Ziyang Tan,Sonia Zicari,Alessandra Ruggiero,Giuseppe Rubens Pascucci,Veronica Santilli,Tessa M. Campbell,Yenan T. Bryceson,Daniel Eriksson,Daniel Eriksson,Jun Wang,Alessandra Marchesi,Tadepally Lakshmikanth,Andrea Campana,Alberto Villani,Paolo Rossi,Paolo Rossi,Nils Landegren,Nils Landegren,Paolo Palma,Paolo Palma,Petter Brodin,Petter Brodin +29 more
TL;DR: The inflammatory response in MIS-C differs from the cytokine storm of severe acute COVID-19, shares several features with Kawasaki disease, but also differs from this condition with respect to T cell subsets, interleukin (IL)-17A, and biomarkers associated with arterial damage.
Posted ContentDOI
The Immunology of Multisystem Inflammatory Syndrome in Children with COVID-19
Camila Rosat Consiglio,Nicola Cotugno,Nicola Cotugno,Fabian Sardh,Christian Pou,Donato Amodio,Donato Amodio,Lucie Rodriguez,Ziyang Tan,Sonia Zicari,Alessandra Ruggiero,Giuseppe Rubens Pascucci,Veronica Santilli,Tessa M. Campbell,Yenan T. Bryceson,Daniel Eriksson,Daniel Eriksson,Jun Wang,Alessandra Marchesi,Tadepally Lakshmikanth,Andrea Campana,Alberto Villani,Paolo Rossi,Paolo Rossi,Nils Landegren,Nils Landegren,Paolo Palma,Paolo Palma,Petter Brodin,Petter Brodin +29 more
TL;DR: The inflammatory response in MIS-C differs from the cytokine storm of severe acute COVID-19, is more similar to Kawasaki disease, but also differ from this with respect to T-cell subsets, IL-17A and biomarkers associated with arterial damage.
Journal ArticleDOI
Bifidobacteria-mediated immune system imprinting early in life.
Bethany M. Henrick,Lucie Rodriguez,Tadepally Lakshmikanth,Christian Pou,Ewa Henckel,Ewa Henckel,Ewa Henckel,Aron Arzoomand,Axel Olin,Jun Wang,Jaromír Mikeš,Ziyang Tan,Yang Chen,Amy M. Ehrlich,Anna Karin Bernhardsson,Constantin Habimana Mugabo,Ylva Ambrosiani,Anna Gustafsson,Anna Gustafsson,Stephanie Chew,Heather Brown,Johann Prambs,Kajsa Bohlin,Kajsa Bohlin,Ryan D. Mitchell,Mark A. Underwood,Jennifer T. Smilowitz,J. Bruce German,Steven A. Frese,Steven A. Frese,Petter Brodin,Petter Brodin +31 more
TL;DR: This article showed that a lack of bifidobacteria, and in particular depletion of genes required for human milk oligosaccharide utilization from the metagenome, is associated with systemic inflammation and immune dysregulation early in life.
Posted ContentDOI
Bifidobacteria-mediated immune system imprinting early in life
Bethany M. Henrick,Lucie Rodriguez,Tadepally Lakshmikanth,Christian Pou,Ewa Henckel,Ewa Henckel,Ewa Henckel,Axel Olin,Jun Wang,Jaromír Mikeš,Ziyang Tan,Yang Chen,Amy M. Ehrlich,Anna Karin Bernhardsson,Constantin Habimana Mugabo,Ylva Ambrosiani,Anna Gustafsson,Anna Gustafsson,Stephanie Chew,Heather Brown,Johann Prambs,Kajsa Bohlin,Kajsa Bohlin,Ryan D. Mitchell,Mark A. Underwood,Jennifer T. Smilowitz,J. Bruce German,Steven A. Frese,Petter Brodin,Petter Brodin +29 more
TL;DR: An ordered sequence of immune changes after birth, driven by microbial interactions is mapped, triggered by microbial colonization that distinguish children with different gut bacterial composition.
Journal ArticleDOI
Systems-Level Immunomonitoring from Acute to Recovery Phase of Severe COVID-19.
Lucie Rodriguez,Pirkka T. Pekkarinen,Tadepally Lakshmikanth,Ziyang Tan,Camilla Rosat Consiglio,Christian Pou,Yang Chen,Constantin Habimana Mugabo,Ngoc Anh Nguyen,Kirsten Nowlan,Tomas Strandin,Lev Levanov,Jaromír Mikeš,Ju Wang,Anu Kantele,Jussi Hepojoki,Olli Vapalahti,Santtu Heinonen,Eliisa Kekäläinen,Petter Brodin,Petter Brodin +20 more
TL;DR: An IFNγ – Eosinophil axis activated prior to lung hyperinflammation and changes in cell-cell coregulation during different stages of the disease are described and map an immune trajectory during recovery that is shared among patients with severe COVID-19.